Status:
COMPLETED
Nasal Continuous Positive Airway Pressure Versus Standard Care During Procedural Sedation for Gastrointestinal Endoscopy
Lead Sponsor:
Johns Hopkins University
Conditions:
Hypoxia
Endoscopy
Eligibility:
All Genders
18-100 years
Phase:
NA
Brief Summary
This study is a randomized controlled trial comparing oxygen delivery by nasal mask with continuous positive airway pressure versus standard care (nasal cannula or standard facemask) during propofol-b...
Detailed Description
This study is a randomized controlled trial comparing oxygen delivery by nasal mask with continuous positive airway pressure versus standard care (nasal cannula or standard facemask) during propofol-b...
Eligibility Criteria
Inclusion
- Adult patients (≥ 18 years of age) undergoing colonoscopy, endoscopic gastroduodenoscopy, and endoscopic gastroduodenoscopy with biopsy and/or ultrasound, or combined upper and lower endoscopy procedure anticipated to last longer than 10 minutes in the Endoscopy Suite at the Johns Hopkins Hospital when the anesthetic plan is monitored anesthesia care with propofol-based anesthesia with a natural airway.
Exclusion
- Left ventricular Assist Device
- Severe Pulmonary Hypertension
- Ejection fraction less than 35 percent
- Active Congestive Heart Failure Exacerbation
- Planned procedure is Balloon Enteroscopy or Endoscopic Retrograde Duodenoscopy.
- Topical lidocaine administration
- Pregnancy
- Previous enrollment in this study
Key Trial Info
Start Date :
October 30 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 23 2019
Estimated Enrollment :
111 Patients enrolled
Trial Details
Trial ID
NCT03369197
Start Date
October 30 2017
End Date
October 23 2019
Last Update
October 18 2022
Active Locations (1)
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1
Johns Hopkins Hospital
Baltimore, Maryland, United States, 21287